Regulatory Affairs CMC Biologicals Role *** Covering the full project lifecycle Manager *** Based in Brussels

Reference: TM280819

Expiry Date: 28-09-2019

Category Regulatory Affairs

Salary: On Application

Job Type: Full Time

Location:
Belgium

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Job Description

Regulatory Affairs CMC Biologicals Role *** Covering the full project lifecycle Manager *** Based in Brussels

We have a new role based in Brussels, Belgium for a Global pharmaceutical company who are now extensively expanding their Global RA CMC team.

My client is a highly rated and extremely successful Bio-Pharmaceutical company with a Global reach.  They are seeking  Regulatory Affairs CMC professionals who have experience in Biologicals  (mAbs, Vaccines, Proteins) for roles that will grow to cover the full project lifecycle, from early phase development to supporting initial MAA’s and global market expansion projects (to include, Japan, China, LatAm and Asia-Pac), whilst maximizing the business benefits balanced with regulatory compliance.

The roles are broad based and varied role and will include further training and development in:

  • Leading, guiding and developing  global RA CMC development strategies
  • Providing CMC focused support for products in late stage development
  • Managing MAA submissions for EU and then later US markets

You will need to have at least 18 months of regulatory affairs CMC experience with a commercial or academic background in Biotechnology. My client is offering a strong salary at the upper end of the pay scale with a number of strong benefits/initiatives around full re-location, private healthcare, sign-on allowance, and strong overall benefits package.

 

To Apply!

To apply for this role, please press the red “Apply for position” button, or contact Theo Moore on +44 (0)207 801 3384 or Oli Dimitrov on +44 (0)207 801 3388 in full confidence to receive more details on this role or to hear about other available opportunities in Regulatory Affairs.

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